| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:166999074-166999415 | Common:1; Rare:116 | ||||
| chr6:169701986-169702334 | Common:5; Rare:152 | ||||
| chr6:169751525-169751658 | Rare:51; Clinvar (benign):2 | ||||
| chr6:170306548-170306814 | Common:2; Rare:88 | ||||
| chr6:170554169-170554420 | Common:1; Rare:74 | ||||
| chr6:170584588-170584773 | Common:1; Rare:61 | ||||
| chr7:192412-192583 | Common:1; Rare:36 | ||||
| chr7:727043-727135 | Rare:22; Clinvar:4 | ||||
| chr7:727220-727314 | Rare:34; Clinvar:2 | ||||
| chr7:975502-975654 | Common:1; Rare:69 | ||||
| chr7:1504323-1504434 | Common:1; Rare:58 | ||||
| chr7:1569998-1570118 | Common:1; Rare:37 | ||||
| chr7:2242165-2242270 | Common:2; Rare:63 | ||||
| chr7:2354573-2354926 | Common:5; Rare:149 | ||||
| chr7:2403290-2403611 | Common:1; Rare:127 |